Muscat R, Montgomery A M, Willner P
Psychology Department, City of London Polytechnic, UK.
Psychopharmacology (Berl). 1989;99(3):402-8. doi: 10.1007/BF00445567.
Feeding elicited by the 5HT1A agonist 8-OH-DPAT was blocked by pretreatment with the DA antagonists SCH-23390 and sulpiride, in two experiments conducted in non-deprived rats and in three experiments conducted after 4 h food deprivation. In deprived animals, 8-OH-DPAT prolonged the initial period of feeding. However, in non-deprived animals, 8-OH-DPAT delayed the onset of eating, and suppressed post-prandial resting; both SCH-23390 and sulpiride restored the normal pattern of behaviour. All three drugs suppressed grooming. The results suggest that 8-OH-DPAT elicits feeding by a secondary disinhibition of activity postsynaptic to DA neurons. The consequences of this mechanism for the interpretation of 8-OH-DPAT-induced feeding are discussed.
在对未禁食大鼠进行的两项实验以及禁食4小时后进行的三项实验中,5-羟色胺1A受体激动剂8-羟基二丙胺基四氢萘(8-OH-DPAT)引发的进食行为被多巴胺拮抗剂SCH-23390和舒必利预处理所阻断。在禁食动物中,8-OH-DPAT延长了进食初期。然而,在未禁食动物中,8-OH-DPAT延迟了进食开始时间,并抑制了餐后静息状态;SCH-23390和舒必利都恢复了正常行为模式。这三种药物都抑制了梳理行为。结果表明,8-OH-DPAT通过对多巴胺能神经元突触后活动的继发性去抑制作用来引发进食。本文讨论了这一机制对解释8-OH-DPAT诱导进食的影响。